Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
External references
Supporting evidence
ID History
- Gene history

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Gene: slc16a5a ENSDARG00000030472

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Description

solute carrier family 16 member 5 [Source:HGNC Symbol;Acc:HGNC:10926]

Location

Chromosome 12: 26,566,422-26,587,231 reverse strand.

GRCz11:CM002896.2

About this gene

This gene has 2 transcripts (splice variants), 240 orthologues and 21 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000153168.2	slc16a5a-202	2157	506aa	ENSDARP00000127291.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	E7FB53	A single transcript chosen for a gene which is the most conserved, most highly expressed, has the longest coding sequence and is represented in other key resources, such as NCBI and UniProt. This is defined in detail on http://www.ensembl.org/info/genome/genebuild/canonical.htmlEnsembl Canonical, APPRIS P1: Transcript(s) expected to code for the main functional isoform based solely on the core modules in the APPRIS. APPRIS is a system to annotate alternatively spliced transcripts based on a range of computational methods to identify the most functionally important transcript(s) of a gene. APPRIS P1,
ENSDART00000045186.6	slc16a5a-201	1658	506aa	ENSDARP00000045185.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	E7FB53	APPRIS P1: Transcript(s) expected to code for the main functional isoform based solely on the core modules in the APPRIS. APPRIS is a system to annotate alternatively spliced transcripts based on a range of computational methods to identify the most functionally important transcript(s) of a gene. APPRIS P1,

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Summary

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